<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8</volume><submitter>McCoy J</submitter><pubmed_abstract>Antiandrogens have demonstrated a protective effect for COVOD-19 patients in observational and interventional studies. The goal of this study was to determine if proxalutamide, an androgen receptor antagonist, could be an effective treatment for men with COVID-19 in an outpatient setting. A randomized, double-blinded, placebo-controlled clinical trial was conducted at two outpatient centers (Brasilia, Brazil). Patients were recruited from October 21 to December 24, 2020 (clinicaltrials.gov number, NCT04446429). Male patients with confirmed COVID-19 but not requiring hospitalization (COVID-19 8-point ordinal scale &lt;3) were administered proxalutamide 200 mg/day or placebo for up to 7 days. The primary endpoint was hospitalization rate at 30 days post-randomization. A total of 268 men were randomized in a 1:1 ratio. 134 patients receiving proxalutamide and 134 receiving placebo were included in the intention-to-treat analysis. The 30-day hospitalization rate was 2.2% in men taking proxalutamide compared to 26% in placebo, &lt;i>P&lt;/i> &lt; 0.001. The 30-day hospitalization risk ratio was 0.09; 95% confidence interval (CI) 0.03-0.27. Patients in the proxalutamide arm more frequently reported gastrointestinal adverse events, however, no patient discontinued treatment. In placebo group, 6 patients were lost during follow-up, and 2 patients died from acute respiratory distress syndrome. Here we demonstrate the hospitalization rate in proxalutamide treated men was reduced by 91% compared to usual care.</pubmed_abstract><journal>Frontiers in medicine</journal><pagination>668698</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8326462</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Proxalutamide Reduces the Rate of Hospitalization for COVID-19 Male Outpatients: A Randomized Double-Blinded Placebo-Controlled Trial.</pubmed_title><pmcid>PMC8326462</pmcid><pubmed_authors>Cadegiani FA</pubmed_authors><pubmed_authors>Sinclair R</pubmed_authors><pubmed_authors>Vano-Galvan S</pubmed_authors><pubmed_authors>Stanimirovic A</pubmed_authors><pubmed_authors>Situm M</pubmed_authors><pubmed_authors>Onety DC</pubmed_authors><pubmed_authors>Kovacevic M</pubmed_authors><pubmed_authors>Goren A</pubmed_authors><pubmed_authors>Shapiro J</pubmed_authors><pubmed_authors>Tosti A</pubmed_authors><pubmed_authors>Dorner E</pubmed_authors><pubmed_authors>Zimerman RA</pubmed_authors><pubmed_authors>McCoy J</pubmed_authors><pubmed_authors>Fonseca D</pubmed_authors><pubmed_authors>Wambier CG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proxalutamide Reduces the Rate of Hospitalization for COVID-19 Male Outpatients: A Randomized Double-Blinded Placebo-Controlled Trial.</name><description>Antiandrogens have demonstrated a protective effect for COVOD-19 patients in observational and interventional studies. The goal of this study was to determine if proxalutamide, an androgen receptor antagonist, could be an effective treatment for men with COVID-19 in an outpatient setting. A randomized, double-blinded, placebo-controlled clinical trial was conducted at two outpatient centers (Brasilia, Brazil). Patients were recruited from October 21 to December 24, 2020 (clinicaltrials.gov number, NCT04446429). Male patients with confirmed COVID-19 but not requiring hospitalization (COVID-19 8-point ordinal scale &lt;3) were administered proxalutamide 200 mg/day or placebo for up to 7 days. The primary endpoint was hospitalization rate at 30 days post-randomization. A total of 268 men were randomized in a 1:1 ratio. 134 patients receiving proxalutamide and 134 receiving placebo were included in the intention-to-treat analysis. The 30-day hospitalization rate was 2.2% in men taking proxalutamide compared to 26% in placebo, &lt;i>P&lt;/i> &lt; 0.001. The 30-day hospitalization risk ratio was 0.09; 95% confidence interval (CI) 0.03-0.27. Patients in the proxalutamide arm more frequently reported gastrointestinal adverse events, however, no patient discontinued treatment. In placebo group, 6 patients were lost during follow-up, and 2 patients died from acute respiratory distress syndrome. Here we demonstrate the hospitalization rate in proxalutamide treated men was reduced by 91% compared to usual care.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2022-02-11T15:42:00.429Z</modification><creation>2022-02-11T15:42:00.429Z</creation></dates><accession>S-EPMC8326462</accession><cross_references><pubmed>34350193</pubmed><doi>10.3389/fmed.2021.668698</doi></cross_references></HashMap>